This information is provided in good faith based on publicly available regulatory information as of 2025. Laws change. Uptide is not a law firm and this is not legal advice. Buyers are solely responsible for ensuring compliance with laws in their jurisdiction.
Shipping by Country
We ship to all EU member states. Regulatory environment varies — read the notes for your country.
Netherlands
Uptide ships from the Netherlands. Research peptides sold as laboratory reference materials are not classified as controlled substances under the Opiumwet. EU medical product regulations (AMG equivalent: Geneesmiddelenwet) apply to products marketed for therapeutic use — Uptide products are sold exclusively for research and are not marketed as medicines.
- Research peptides not listed on the Opiumwet are not controlled substances.
- Not marketed as medicines, so Geneesmiddelenwet does not apply.
- Purchasing for personal therapeutic use falls on the buyer's legal responsibility.
Germany
Germany applies the Arzneimittelgesetz (AMG) strictly. A compound can be classified as a medicine if it is intended for therapeutic use or has an implied therapeutic function — even without explicit marketing claims. Purchasing peptides for anything other than genuine scientific research creates legal risk for the buyer. We ship to Germany only for legitimate research purposes.
- AMG §2 classifies substances by intended use — if therapeutic intent is implied, AMG applies.
- Tirzepatide (Mounjaro®) is an approved prescription drug in Germany — buyers must confirm research purpose.
- GHRP peptides are not separately scheduled but their research use must be documented.
- Melanotan II has been subject to enforcement action in Germany — we do not ship MT-II to Germany.
Belgium
Belgium's FAMHP (Federal Agency for Medicines and Health Products) regulates medicines, but research compounds not marketed as medicines and not on the controlled substances list fall outside their scope. Most peptides in our catalogue can be ordered for research purposes.
- FAMHP jurisdiction covers medicines — compounds marketed only for research are outside scope.
- Belgian customs may query shipments — attach proof of research purpose if requested.
France
France's ANSM (Agence nationale de sécurité du médicament) has a broad interpretation of what constitutes a médicament. Compounds that could be considered to have a pharmacological effect may fall under pharmaceutical regulation even if sold as research substances. We ship to France but buyers should verify their institution's import policy.
- ANSM may classify peptides as médicaments if physiological effect can be demonstrated.
- Semaglutide is a prescription médicament in France — we do not sell it as a product to France.
- Institutional buyers (universities, labs) typically have import clearance frameworks in place.
- Private individuals ordering peptides face the highest regulatory scrutiny.
Spain
Spain's AEMPS (Agencia Española de Medicamentos y Productos Sanitarios) regulates medicines. Research peptides not listed as controlled substances and not marketed as medicines are generally importable for laboratory use. Spain has a relatively clear research exemption for scientific institutions.
- AEMPS regulates medicines — not compounds explicitly sold for laboratory research only.
- No specific peptide scheduling in Spanish law outside of approved medicines.
Italy
AIFA (Agenzia Italiana del Farmaco) governs pharmaceutical products in Italy. Research peptides sold strictly for laboratory use are not classified as medicinal products. Customs may hold shipments for inspection.
- AIFA jurisdiction applies to medicinal products — research materials fall outside this scope.
- Customs delays occur occasionally; documentation of research use is recommended.
Sweden
Sweden's Läkemedelsverket (Medical Products Agency) has one of the strictest interpretations in the EU. Many peptides that are freely available for research in other EU countries are classified as läkemedel (medicines) in Sweden. We ship only a limited subset of compounds to Sweden and strongly recommend buyers consult Swedish law before ordering.
- Läkemedelsverket has classified multiple research peptides as prescription medicines.
- Importation without prescription may constitute a criminal offence under Läkemedelslagen.
- GH-axis peptides (GHRH analogues, GHRPs) are particularly restricted.
- BPC-157, GHK-Cu, and NAD+ are generally unaffected by Swedish medicine law.
Austria
Austria's BASG (Bundesamt für Sicherheit im Gesundheitswesen) applies the Arzneimittelgesetz similar to Germany. Growth hormone secretagogues and GLP-1 analogues face stricter scrutiny. Research use for institutional labs is generally permitted.
- AMG classification may apply to peptides with pharmacological activity even without marketing as medicines.
- Semaglutide and Retatrutide require prescription in Austria — not sold for personal use.
- Research institutions can typically import under a research exemption.
Denmark
Denmark's Lægemiddelstyrelsen (DKMA) regulates medicines. Most peptides sold as research materials are outside the scope of Danish pharmaceutical law. Denmark has historically been permissive regarding research chemical imports.
- Research compounds not scheduled under Danish law are freely importable for lab use.
- Approved drugs (Semaglutide) require prescription regardless.
Poland
Poland's Urząd Rejestracji applies EU pharmaceutical directives. Most research peptides fall outside the scope of medicine regulation when sold strictly for research. Poland has a well-developed scientific research sector and is a common destination for research compounds.
- No specific peptide scheduling beyond standard EU pharmaceutical law.
- Research use with institutional documentation is straightforward.
Czech Republic
SUKL (State Institute for Drug Control) applies EU pharmaceutical directives. Research peptides not classified as medicines under SÚKL are importable for scientific research purposes.
- Standard EU pharmaceutical directive applies — research compounds not on SÚKL's medicine list are permissible.
Compound-Specific Regulatory Notes
Risk classification is relative to research use in the EU. HIGH means legal risk exists even for research purposes in some countries. LOW means compound is clearly within research-only legal scope across most EU countries.
Retatrutide
MEDIUM RISKInvestigational GLP-1/GIP/glucagon triple agonist (phase III trials as of 2025). Not approved as a medicine in the EU. Classification as a medicine-in-development may apply in some countries. Legal to purchase for scientific research at this stage.
Melanotan II
MEDIUM RISKNot scheduled as a controlled substance in most EU countries, but has been subject to enforcement in Germany and the Netherlands due to product liability concerns when sold for cosmetic use. Uptide sells strictly for research. Not shipped to Germany.
Tesamorelin
MEDIUM RISKApproved as Egrifta® in the US for HIV-associated lipodystrophy. No EMA approval in the EU as of 2025. Legal as a research compound in most EU countries, though AMG/Läkemedelsverket classification may apply in DE/SE.
HGH Somatropin
MEDIUM RISKRecombinant human growth hormone. Approved as a prescription medicine throughout the EU under various brand names. Buying without a prescription creates legal risk in all EU member states. Uptide sells for research purposes only — buyers must confirm research context.
Oxytocin
MEDIUM RISKApproved pharmaceutical in the EU (obstetrics/labour induction). Not a controlled substance for research purposes but carries prescription-medicine classification risk in some countries. Research use for non-clinical laboratory studies is generally permissible.
BPC-157
LOW RISKNo regulatory approval in any EU country. Clearly a research compound. Low regulatory risk throughout the EU as long as sold for laboratory use with appropriate disclaimers.
TB-500 (Thymosin β4)
LOW RISKNo EU marketing authorisation. Banned by WADA for use in sport (in-competition and out-of-competition). Legal for laboratory research. Not relevant for human use without prescription.
GHK-Cu
LOW RISKUsed in cosmetic formulations under EU Cosmetics Regulation. As a research compound it is clearly within legal bounds. Lowest regulatory risk of any compound in the catalogue.
IGF-1 LR3
LOW RISKBanned by WADA. No EU marketing authorisation. Research use is legal throughout the EU. Enforcement attention due to misuse in sport.
CJC-1295 (with/without DAC)
LOW RISKGHRH analogues. No EU marketing authorisation. Research compounds. WADA-banned. Legal for laboratory use across the EU.
GHRP-2 / GHRP-6 / Ipamorelin
LOW RISKGH secretagogues. No EU scheduling. WADA-banned substances. Legal for scientific research. Sweden may classify these under Läkemedelslagen.
Semax / Selank
LOW RISKNootropic peptides registered as medicines in Russia and some CIS countries but not in the EU. No EU controlled substance scheduling. Legal to purchase for research.
Sermorelin
LOW RISKGHRH analogue. Not approved in the EU. WADA-banned. No EU scheduling. Legal for laboratory research throughout the EU.
MOTS-C
LOW RISKMitochondrial-derived peptide. No EU marketing authorisation, no scheduling. Clear research compound with no known regulatory enforcement history in the EU.
NAD+ (Nicotinamide Adenine Dinucleotide)
LOW RISKNot a medicine. Available as a dietary supplement in many EU countries. No scheduling or restriction concerns. Lowest regulatory risk in the catalogue.
Questions about your country?
Contact us directly with your jurisdiction and research context. We will tell you whether we can ship and what documentation may be required.